Congenital hypomyelination due to myelin protein zero Q215X mutation
P. Mandich, G. L. Mancardi, A. Varese, S. Soriani, E. Di Maria, E. Bellone, M. Bado, L. Gross, A. J. Windebank, F. Ajmar, A. SchenoneVolume:
45
Année:
1999
Langue:
english
Pages:
3
DOI:
10.1002/1531-8249(199905)45:53.0.co;2-k
Fichier:
PDF, 4.60 MB
english, 1999